JP2009502862A - 殺菌剤５−アルキル−６−フェニルピラゾロピリミジン−７−イルアミン - Google Patents
殺菌剤５−アルキル−６−フェニルピラゾロピリミジン−７−イルアミン Download PDFInfo
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- JP2009502862A JP2009502862A JP2008523330A JP2008523330A JP2009502862A JP 2009502862 A JP2009502862 A JP 2009502862A JP 2008523330 A JP2008523330 A JP 2008523330A JP 2008523330 A JP2008523330 A JP 2008523330A JP 2009502862 A JP2009502862 A JP 2009502862A
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- 239000003899 bactericide agent Substances 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 122
- 239000000203 mixture Substances 0.000 claims abstract description 30
- 238000000034 method Methods 0.000 claims abstract description 11
- -1 C 1 -C 10 -alkyl Chemical group 0.000 claims description 158
- 229910052736 halogen Inorganic materials 0.000 claims description 18
- 150000002367 halogens Chemical class 0.000 claims description 18
- 241000233866 Fungi Species 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
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- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
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- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 4
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- 125000005842 heteroatom Chemical group 0.000 claims description 4
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- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 3
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
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- 125000005865 C2-C10alkynyl group Chemical group 0.000 claims description 2
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- CCVZGXADPRHPCG-UHFFFAOYSA-N 5-ethyl-6-(4-ethylphenyl)-2-methyl-1h-pyrazolo[4,3-d]pyrimidin-7-amine Chemical compound CCC1=NC2=CN(C)NC2=C(N)N1C1=CC=C(CC)C=C1 CCVZGXADPRHPCG-UHFFFAOYSA-N 0.000 description 4
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- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 4
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
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- UFHLMYOGRXOCSL-UHFFFAOYSA-N isoprothiolane Chemical compound CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1 UFHLMYOGRXOCSL-UHFFFAOYSA-N 0.000 description 1
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- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
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- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 description 1
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 125000004305 thiazinyl group Chemical group S1NC(=CC=C1)* 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005035689 | 2005-07-27 | ||
| PCT/EP2006/064465 WO2007012600A1 (de) | 2005-07-27 | 2006-07-20 | Fungizide 5-alkyl-6-phenyl-pyrazolopyrimidin-7-ylamine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2009502862A true JP2009502862A (ja) | 2009-01-29 |
Family
ID=37401069
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008523330A Withdrawn JP2009502862A (ja) | 2005-07-27 | 2006-07-20 | 殺菌剤５−アルキル−６−フェニルピラゾロピリミジン−７−イルアミン |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20090156398A1 (de) |
| EP (1) | EP1910372A1 (de) |
| JP (1) | JP2009502862A (de) |
| CN (1) | CN101228170A (de) |
| BR (1) | BRPI0613941A2 (de) |
| WO (1) | WO2007012600A1 (de) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009529054A (ja) * | 2006-03-08 | 2009-08-13 | ノバルティス アクチエンゲゼルシャフト | 神経障害の処置におけるピラゾロ［１，５ａ］ピリミジン−７−イルアミン誘導体の使用 |
| AU2008206921B2 (en) * | 2007-01-19 | 2012-11-01 | Basf Se | Fungicidal mixtures of 1-methylpyrazole-4-ylcarboxylic acid anilides and azolopyrimidinylamines |
| JP5351047B2 (ja) * | 2007-01-30 | 2013-11-27 | ビーエーエスエフ ソシエタス・ヨーロピア | アゾロピリミジニルアミン誘導体及び殺虫剤を主成分とする殺虫性混合物 |
| EP2192841A2 (de) | 2007-09-20 | 2010-06-09 | Basf Se | Zusammensetzungen mit einem fungiziden stamm und mindestens einem zusätzlichen fungizid |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3130633A1 (de) * | 1981-08-01 | 1983-02-17 | Basf Ag, 6700 Ludwigshafen | 7-amino-azolo(1,5-a)pyrimidine und diese enthaltende fungizide |
| DE3338292A1 (de) * | 1983-10-21 | 1985-05-02 | Basf Ag, 6700 Ludwigshafen | 7-amino-azolo(1,5-a)-pyrimidine und diese enthaltende fungizide |
| JP2002308879A (ja) * | 2001-04-13 | 2002-10-23 | Nippon Soda Co Ltd | ５−ハロアルキル−アゾロピリミジン化合物、製造方法及び有害生物防除剤 |
| DE10223917A1 (de) * | 2002-05-29 | 2003-12-11 | Bayer Cropscience Ag | Pyrazolopyrimidine |
| CA2527136A1 (en) * | 2003-06-03 | 2004-12-09 | Basf Aktiengesellschaft | Substituted pyrazolopyrimidines, methods for the production thereof, use of the same for controlling pathogenic fungi, and agents containing said compounds |
| DE10357567A1 (de) * | 2003-12-10 | 2005-07-07 | Bayer Cropscience Ag | Pyrazolopyrimidine |
| DE10359445A1 (de) * | 2003-12-17 | 2005-07-28 | Enginion Ag | Wasserstoff-Verbrennungsmotor |
| CN1894253A (zh) * | 2003-12-17 | 2007-01-10 | 巴斯福股份公司 | 6－五氟苯基三唑并嘧啶、其制备方法及其在防治病原性真菌中的用途以及包含所述物质的组合物 |
-
2006
- 2006-07-20 US US11/996,780 patent/US20090156398A1/en not_active Abandoned
- 2006-07-20 JP JP2008523330A patent/JP2009502862A/ja not_active Withdrawn
- 2006-07-20 CN CNA2006800269952A patent/CN101228170A/zh active Pending
- 2006-07-20 EP EP06777864A patent/EP1910372A1/de not_active Withdrawn
- 2006-07-20 BR BRPI0613941A patent/BRPI0613941A2/pt not_active IP Right Cessation
- 2006-07-20 WO PCT/EP2006/064465 patent/WO2007012600A1/de active Application Filing
Also Published As
| Publication number | Publication date |
|---|---|
| EP1910372A1 (de) | 2008-04-16 |
| BRPI0613941A2 (pt) | 2016-11-22 |
| US20090156398A1 (en) | 2009-06-18 |
| CN101228170A (zh) | 2008-07-23 |
| WO2007012600A1 (de) | 2007-02-01 |
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